NDC 45963-142 – Bupropion Hydrochloride
Bupropion Hydrochloride 300 mg/1 · Tablet, Extended Release · Oral
Product NDC45963-142
Product details
- Brand name
- Bupropion Hydrochloride
- Generic name
- Bupropion Hydrochloride
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077285
- Marketed since
- February 17, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Aminoketone
Active ingredients
- Bupropion Hydrochloride 300 mg/1
Uses, dosage, side effects and warnings for Bupropion hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 45963-142-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (45963-142-05) | May 19, 2015 |
| 45963-142-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (45963-142-30) | Feb 17, 2015 |
| 45963-142-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (45963-142-90) | Jun 15, 2015 |
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